FDA 510(k) Applications Submitted by JASON BLAIN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K040276	02/05/2004	QUANTUM CEMENT RESTRICTOR	QUANTUM ORTHOPEDICS
K050449	02/22/2005	QUANTUM VERTEBRAL BODY REPLACEMENT	QUANTUM ORTHOPEDICS, INC.
K060491	02/24/2006	QUANTUM ANTERIOR CERVICAL PLATE SYSTEM	QUANTUM ORTHOPEDICS, INC.
K141372	05/27/2014	MERCURY SPINAL SYSTEM	SPINAL ELEMENTS, INC.
K991882	06/02/1999	NEXFLEX TOTAL KNEE SYSTEM	NEXMED, INC.
K061576	06/07/2006	MODIFICATION TO QUANTUM VERTEBRAL BODY REPLACEMENT SYSTEM	QUANTUM ORTHOPEDICS, INC.
K992350	07/14/1999	PYLON INTRAMEDULLAARY NAIL SYSTEM	ALPHATEC MFG., INC.
K052641	09/26/2005	MODIFICATION TO: QUANTUM VERTEBRAL BODY REPLACEMENT	QUANTUM ORTHOPEDICS, INC.
K993513	10/18/1999	DELTALOC ANTERIOR CERVICAL PLATE SYSTEM	ALPHATEC MFG., INC.
K993873	11/15/1999	ALPHATEC EXTERNAL FIXATION SYSTEM COMPRESSION/DISTRACTION ROD	ALPHATEC MFG., INC.